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    The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010. by Chen Gao, Qi Shi, Chan Tian, Cao Chen, Jun Han, Wei Zhou, Bao-Yun Zhang, Hui-Ying Jiang, Jin Zhang, Xiao-Ping Dong

    Published 2011-01-01
    “…Polymorphisms of codon 129 in PRNP of the notified cases revealed a highly predominant M129M genotype in Han Chinese. Among 23 genetic human prion diseases, ten were D178N/M129M Fatal familial insomnia (FFI) and five were T188K genetic CJD (gCJD), possibly indicating a special distribution of gCJD-related mutations in Han Chinese. …”
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